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Are there differential symptom profiles that improve in response to different pharmacological treatments of premenstrual syndrome/premenstrual dysphoric disorder?

Halbreich, Uriel (författare)
O'Brien, P M Shaughn (författare)
Eriksson, Elias, 1956 (författare)
Gothenburg University,Göteborgs universitet,Institutionen för neurovetenskap och fysiologi, sektionen för farmakologi,Institute of Neuroscience and Physiology, Department of Pharmacology
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Bäckström, Torbjörn (författare)
Umeå universitet,Obstetrik och gynekologi
Yonkers, Kimberly A (författare)
Freeman, Ellen W (författare)
visa färre...
 (creator_code:org_t)
2006
2006
Engelska.
Ingår i: CNS drugs. - 1172-7047. ; 20:7, s. 523-47
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
Stäng  
  • Current evidence suggests that the accepted treatments for premenstrual syndrome (PMS)/premenstrual dysphoric disorder (PMDD) have similar overall efficacy. While these treatments are more effective than placebo, response rates associated with them are far from satisfactory (<60%), such that, irrespective of treatment modality, there remain a significant number of women who are unresponsive to current conventional pharmacological therapy. The available data on response rates of specific types of premenstrual symptoms to, or symptom profiles that are most amenable to, each treatment modality are limited and not well defined because most studies were not designed to assess specific symptom profiles. Those studies that have attempted to evaluate which symptom profiles respond to specific therapies have revealed variations within the individual modalities, as well as between the different modalities. It appears that suppression of ovulation ameliorates a broad range of behavioural as well as physical premenstrual symptoms. SSRIs are most effective for irritability and anxiety symptoms, with lesser efficacy for 'atypical' premenstrual symptoms. GABAergic compounds are most efficacious for anxiety and anxious/depressive symptoms, while dopamine agonists, particularly bromocriptine, are perhaps most efficacious for mastalgia. Overall treatment response rates may improve if treatments are targeted at well-defined subgroups of patients. Re-analysis of available datasets from randomised clinical trials may shed more light on the notion that targeting women with specific premenstrual symptom profiles for specific treatment modalities would improve response rates beyond the current ceiling of approximately 60%. Such information would also improve understanding of the putative pathophysiological mechanisms underlying PMS and PMDD, and may point to a more specific diagnosis of these conditions.

Ämnesord

MEDICIN OCH HÄLSOVETENSKAP  -- Medicinska och farmaceutiska grundvetenskaper -- Fysiologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Basic Medicine -- Physiology (hsv//eng)

Nyckelord

Central Nervous System
drug effects
physiopathology
Drug Therapy
Combination
Estrogen Antagonists
therapeutic use
Female
Gonadotropin-Releasing Hormone
agonists
Humans
MEDLINE
statistics & numerical data
Meta-Analysis
Ovariectomy
methods
Premenstrual Syndrome
classification
drug therapy
physiopathology
surgery
Randomized Controlled Trials
Serotonin Uptake Inhibitors
therapeutic use
Central Nervous System/drug effects/physiopathology

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